Volume 37, Issue 3 pp. 177-198
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One-bead–one-structure combinatorial libraries

Michal Lebl

Michal Lebl

Selectide Corporation, 1580 E. Hanley Blvd., Tucson, AZ 85737

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Viktor Krchňák

Viktor Krchňák

Selectide Corporation, 1580 E. Hanley Blvd., Tucson, AZ 85737

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Nikolai F. Sepetov

Nikolai F. Sepetov

Selectide Corporation, 1580 E. Hanley Blvd., Tucson, AZ 85737

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Bruce Seligmann

Bruce Seligmann

Selectide Corporation, 1580 E. Hanley Blvd., Tucson, AZ 85737

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Peter Štrop

Peter Štrop

Selectide Corporation, 1580 E. Hanley Blvd., Tucson, AZ 85737

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Stephen Felder

Stephen Felder

Selectide Corporation, 1580 E. Hanley Blvd., Tucson, AZ 85737

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Kit S. Lam

Kit S. Lam

Arizona Cancer Center and Department of Medicine, University of Arizona, College of Medicine, Tucson, AZ 85724

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First published: 1995
Citations: 124

Abstract

Combinatorial libraries employing the one-bead–one-compound technique are reviewed. Two distinguishing features characterize this technique. First, each compound is identified with a unique solid support, enabling facile segregation of active compounds. Second, the identity of a compound on a positively reacting bead is elucidated only after its biological relevance is established. Direct methods of structure identification (Edman degradation and mass spectroscopy) as well as indirect “coding” methods facilitating the synthesis and screening of nonpeptide libraries are discussed. Nonpeptide and “scaffold” libraries, together with a new approach for the discovery of a pentide binding motif using a “library of libraries,” are also discussed. In addition, the ability to use combinatorial libraries to optimize initially discovered leads is illustrated with examples using peptide libraries. © 1994 John Wiley & Sons, Inc.

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